US4539395A - Film-forming composition comprising chlorinated polyalkylene glycol - Google Patents
Film-forming composition comprising chlorinated polyalkylene glycol Download PDFInfo
- Publication number
- US4539395A US4539395A US06/573,994 US57399484A US4539395A US 4539395 A US4539395 A US 4539395A US 57399484 A US57399484 A US 57399484A US 4539395 A US4539395 A US 4539395A
- Authority
- US
- United States
- Prior art keywords
- film
- forming composition
- chlorinated
- solvent
- polyalkyleneglycol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D171/00—Coating compositions based on polyethers obtained by reactions forming an ether link in the main chain; Coating compositions based on derivatives of such polymers
- C09D171/02—Polyalkylene oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/323—Polymers modified by chemical after-treatment with inorganic compounds containing halogens
- C08G65/3233—Molecular halogen
Definitions
- This invention concerns a film-forming composition containing as an effective component a product of the chlorination of polyethyleneglycol (hereinafter abbreviated to as PEG) and/or polypropyleneglycol (hereinafter abbreivated to as PPG)
- PEG polyethyleneglycol
- PPG polypropyleneglycol
- these plastic materials are non-polar substances, and in contrast to paper, they exhibit poor adhesiveness to inks or other film-forming agents. Accordingly, in order to improve the adhesiveness of the printing inks or other film-forming agents, it has been the practice to activate the surface of the above plastic materials to improve its adhesiveness to the ink through treatment of the surface by process such as corona discharge treatment, high frequency discharge treatment, chemical treatment with bichromate or the like.
- binders of the printing inks or other film-forming agents for these treated plastic materials cyclized rubber, polyamide and, nitrocellulose were usually used, but because of unevenness of the treatment and other difficulties, even when applied to the aforesaid treated films, these binders are not satisfactory.
- chlorinated polypropylene soluble in aromatic solvents has appeared as a binder having a good adhesiveness, but it exhibits little solubility in aliphatic solvents or alcohols, and hence, its application has been limited as a binder used for film-forming agent in printing inks or the like.
- the film-forming compositions of the invention contain as binder components the products of the uniform chlorination of PEG, PPG or mixture thereof dissolved in a chlorine-resistant solvent to a chlorine content of 50 to 75% by weight, based upon the weight of the chlorinated products.
- the molecular weight of said PEG or PEG should be above 200.
- chlorinated products are soluble in aliphatic solvents or alcohols as well as in aromatic solvents, they may be applicable either as film-forming compositions used in printing inks or the like for polyolefins, polyesters and others or as modifiers of the hitherto known film-forming agents used in printing inks or the like.
- Chlorinated PEG and chlorinated PPG of the invention are manufactured as follows. PEG or PPG having a molecular weight of more than 200 is dissolved uniformly into a chlorine-resistant solvent such as carbon tetrachloride, with or without the application of pressure. Chlorine gas is passed through this solution to a point where the chlorine content exceeds 50% by weight maintaining a uniformly dissolved state from beginning to end. The reaction proceeds smoothly and is over in a short period, if an organic peroxide, a diazo compound or other compounds used generally as a catalyst for chlorination is present, or ultraviolet rays or if radiation are employed as catalysts.
- a chlorine-resistant solvent such as carbon tetrachloride
- the reason why the molecular weight of PEG or PPG is restricted to above 200 is due to the fact that, if the molecular weight is less than 200, the resulting chlorinated product is so tacky that the drying property of the printing ink using this chlorinated product becomes inferior.
- the chlorine content must be within a range of 50 to 75% by weight because a chlorine content lower than 50% by weight, results is poor storage stability of the product, and 75% by weight is the upper limit of chlorination.
- the chlorinated polymers obtained through the uniform chlorination in a chlorine-resistant solvent as described above do not need to be isolated, and the solvent may be displaced with a chosen solvent (for example, combinations of aromatic solvents aliphatic solvents, alcohols or the like) by direct solvent displacement to convert to binder solutions in solvents for printing inks.
- a chosen solvent for example, combinations of aromatic solvents aliphatic solvents, alcohols or the like
- the chlorinated polymers may be isolated from the chlorine-resistant solvent by steam distillation and then dissolved into the chosen solvent.
- gravure ink was prepared according to the following formulation.
- Varnish for gravure printing having the following composition was prepared by the addition of B, C, F or H in Example 1 or 2 mentioned above to a nitrocellulose varnish.
- each varnish was coated on the plastic films to form a 5 to 7 ⁇ film thickness. This was dried sufficiently at a room temperature and a performance test was carried out. Results are shown in Table 3.
- the polymers of this invention were found to have an excellent adhesiveness and solubility into solvents. Such polymers were never recognized in the past as suitable for printing ink compositions for use on polyolefins.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Wood Science & Technology (AREA)
- Engineering & Computer Science (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyethers (AREA)
- Paints Or Removers (AREA)
Abstract
A film-forming composition containing a chlorinated polyolefinglycol as a binder component which is obtained by uniformly chlorinating in solution polyethyleneglycol and/or polypropyleneglycol having a molecular weight not lower than 200 to a chlorine content of 50-75% by weight.
Description
This invention concerns a film-forming composition containing as an effective component a product of the chlorination of polyethyleneglycol (hereinafter abbreviated to as PEG) and/or polypropyleneglycol (hereinafter abbreivated to as PPG) With the progress of petrochemistry in recent years the demand for, plastic films such as polypropylene film or polyethylene film, and sheets or moldings of such plastics has been increasing steadily.
With this increase, the demand for printing inks or other film-forming agents applicable to these plastic materials has increased, and hence various studies on the subject have been carried out.
However, as is generally well known, these plastic materials are non-polar substances, and in contrast to paper, they exhibit poor adhesiveness to inks or other film-forming agents. Accordingly, in order to improve the adhesiveness of the printing inks or other film-forming agents, it has been the practice to activate the surface of the above plastic materials to improve its adhesiveness to the ink through treatment of the surface by process such as corona discharge treatment, high frequency discharge treatment, chemical treatment with bichromate or the like.
As binders of the printing inks or other film-forming agents for these treated plastic materials, cyclized rubber, polyamide and, nitrocellulose were usually used, but because of unevenness of the treatment and other difficulties, even when applied to the aforesaid treated films, these binders are not satisfactory. Also, in recent years, chlorinated polypropylene soluble in aromatic solvents has appeared as a binder having a good adhesiveness, but it exhibits little solubility in aliphatic solvents or alcohols, and hence, its application has been limited as a binder used for film-forming agent in printing inks or the like.
We have investigated from different angles to overcome the defects of the film-forming compositions used in printing inks or the like for use on the surface of the above-mentioned publicly known polyolefins, and have found that the compositions of the invention have an excellent adhesiveness as the film-forming compositions used in printing inks or the like for polyolefins, and have completed the present invention. The film-forming compositions of the invention contain as binder components the products of the uniform chlorination of PEG, PPG or mixture thereof dissolved in a chlorine-resistant solvent to a chlorine content of 50 to 75% by weight, based upon the weight of the chlorinated products. The molecular weight of said PEG or PEG should be above 200. As these chlorinated products are soluble in aliphatic solvents or alcohols as well as in aromatic solvents, they may be applicable either as film-forming compositions used in printing inks or the like for polyolefins, polyesters and others or as modifiers of the hitherto known film-forming agents used in printing inks or the like.
With regard to the chlorination of PEG or PPG, none of the physical properties of the chlorinated products have been known up to this time, except for a report which describes that high degrees of chlorination may be possible in the dark at room temperature using polyazine containing a conjugated system as a catalyst.
As a result of extensive experiments on the chlorination of PEG or PPG, we have discovered that uniformly chlorinated products having a chosen chlorine content can be obtained by passing the chlorine gas through a carbon tetrachloride solution in which PEG or PPG is completely dissolved, with or without the application of pressure. Moreover, by inspecting their various properties, it was found that, among the uniformly chlorinated polymers mentioned above, those having a chlorine content of 50 to 75% by weight exhibit a particularly therefor desirable adhesiveness to the surface of polyolefins, and that their solubilities were simultaneously superior. On the basis of these findings, we have completed the invention and provide them as film-forming compositions used in printing inks or the like.
In the following, details are given of an application of the invention to the composition of printing ink. Chlorinated PEG and chlorinated PPG of the invention are manufactured as follows. PEG or PPG having a molecular weight of more than 200 is dissolved uniformly into a chlorine-resistant solvent such as carbon tetrachloride, with or without the application of pressure. Chlorine gas is passed through this solution to a point where the chlorine content exceeds 50% by weight maintaining a uniformly dissolved state from beginning to end. The reaction proceeds smoothly and is over in a short period, if an organic peroxide, a diazo compound or other compounds used generally as a catalyst for chlorination is present, or ultraviolet rays or if radiation are employed as catalysts. The reason why the molecular weight of PEG or PPG is restricted to above 200 is due to the fact that, if the molecular weight is less than 200, the resulting chlorinated product is so tacky that the drying property of the printing ink using this chlorinated product becomes inferior. The chlorine content must be within a range of 50 to 75% by weight because a chlorine content lower than 50% by weight, results is poor storage stability of the product, and 75% by weight is the upper limit of chlorination.
The chlorinated polymers obtained through the uniform chlorination in a chlorine-resistant solvent as described above do not need to be isolated, and the solvent may be displaced with a chosen solvent (for example, combinations of aromatic solvents aliphatic solvents, alcohols or the like) by direct solvent displacement to convert to binder solutions in solvents for printing inks. Suitable on the other hand, the chlorinated polymers may be isolated from the chlorine-resistant solvent by steam distillation and then dissolved into the chosen solvent.
In the following, the invention is illustrated by examples, but the scope of the invention is not limited to the examples.
400 g of PEG having a molecular weight of 300 or 20,000 was uniformly dissolved into 10 liter of carbon tetrachloride under the conditions of temperature of 110° C. and pressure of 2 kg/cm2. After air purging, it was chlorinated by introducing chlorine in gas from the bottom of the reaction vessel and irradiating with ultraviolet rays. Chlorinated reaction solutions were drawn out at the desired chlorine content of 50 to 75% by weight and converted to 80% toluene solutions by the solvent displacement method.
400 g of PPG having a molecular weight of 4,000 was uniformly dissolved into 10 l of carbon tetrachloride at a temperature of 78° C. under atmospheric pressure. After air-purging, it was chlorinated by introducing gaseous chlorine from the bottom of the reaction vessel and irradiating with ultraviolet rays. Chlorinated reaction solutions were drawn out at the desired chlorine content of 50 to 65% by weight and converted to 80% toluene solutions by the solvent displacement method.
The chlorine content and the solution viscosity measured on the products in Example 1 and 2 are shown in Table 1.
TABLE 1
______________________________________
Example
EXAMPLE 1 EXAMPLE 2
PEG PEG
(M.W. 300)
(M.W. 20000) PPG (M.W. 4000)
Measurement
A B C D E F G H
______________________________________
Chlorine 53.2 63.8 52.3 65.9 70.4 50.8 60.5 65.0
Content (%)
Solution 290 200 1440 890 760 570 410 350
Viscosity
(CPS)
______________________________________
Solution viscosity: Viscosity of 80% toluene solution in centipoise at
25° C.
Using Samples A, D or G in Example 1 or 2 mentioned above, gravure ink was prepared according to the following formulation.
______________________________________
Varnish (A, D or G in Example 1 or 2)
30
Pigment (Carmine 6BN) 10
Solvent (toluene) Corrective quantity
α
for a fixed viscosity
40 + α
______________________________________
(Note)
Carmine 6BN: from Toyo Ink Manufacturing Co.
After milling for 2 hours with sand mill, the viscosity was adjusted to 20±2 seconds by using zahn cup No. 5. Each ink was coated individually on the plastic films to form a 5 to 7μ ink film. After drying sufficiently at room temperature, a performance test was carried out. Results are shown in Table 2 which includes results obtained with comparative Examples, (cyclized rubber and chlorinated polypropylene).
TABLE 2
__________________________________________________________________________
Physical Property
Difficulty
Storage-
Oil Resistance
Blocking
in stability
resistance
Adhesiveness
to crumpling
property
inking
of ink
of ink
○4
○5
○6
Sample ○1
○2
○3
PP PET PP PET PP
PET
__________________________________________________________________________
Example
A Easy Normal
Excellent
⊚
⊚
⊚
○
⊚
⊚
D " " " ⊚
⊚
⊚
○
⊚
⊚
G " " " ⊚
⊚
⊚
○
⊚
⊚
Comparative
Example
Cyclized
" Apt to
Bad X X X X X X
rubber galation
Chlori-
" Apt to
Good ⊚
X ⊚
X ⊚
X
nated poly- galation
propylene
__________________________________________________________________________
Varnish for gravure printing having the following composition was prepared by the addition of B, C, F or H in Example 1 or 2 mentioned above to a nitrocellulose varnish.
______________________________________
Chlorinated product (B, C, F or H in Example 1
0.8
or 2 or chlorinated polypropylene)
Nitrocellulose (H 1/8) 2.0
MEK 9.0
Toluene 5.6
IPA 3.6
21.0
______________________________________
After blending homogeneously, each varnish was coated on the plastic films to form a 5 to 7μ film thickness. This was dried sufficiently at a room temperature and a performance test was carried out. Results are shown in Table 3.
TABLE 3
__________________________________________________________________________
Physical property
Difficulty Storage
Oil-resis- Resistance
in making stability
tance of
Adhesiveness
to crumpling
Blocking
varnish of varnish
varnish
○4
○5
Property ○6
Sample
○1
○2
○3
PP PET PP PET PP PET
__________________________________________________________________________
Example
B Easy Normal
Excellent
⊚
○
⊚
○
⊚
⊚
C " " " ⊚
○
⊚
○
⊚
⊚
F " " " ⊚
○
⊚
○
⊚
⊚
H " " " ⊚
○
⊚
○
⊚
⊚
Comparative
Example
Chlorinated
" Seperate
-- -- -- -- -- -- --
Polypro-
pylene
Nitrocellu-
-- -- Excellent
Δ
X Δ
X ⊚
⊚
lose
varnish
__________________________________________________________________________
Conditions and judgement are the same as those in Example 3
Comparison of the solubility into toluene/alcohol solvents:
______________________________________
Toluene/Ethanol
Sample 9/1 8/2 7/3 5/5
______________________________________
G in Example 2
clear clear clear slightly
cloudy
Chlorinated clear slightly deposit
deposit
Polypropylene cloudy
______________________________________
Chlorinated polypropylene used is the same as that in Example 3
From the results in Example 3, 4 and 5 mentioned above, the polymers of this invention were found to have an excellent adhesiveness and solubility into solvents. Such polymers were never recognized in the past as suitable for printing ink compositions for use on polyolefins.
Claims (7)
1. A film-forming composition comprising a chlorinated polyalkyleneglycol binder produced by chlorinating a polyalkyleneglycol having a molecular weight of not less than 200 and selected from the group consisting of polyethyleneglycol, polypropyleneglycol and mixtures thereof in a solution of the polyalkyleneglycol in a chlorine-resistant solvent, to a chemically combined chlorine content of 50 to 75% by weight, based upon the weight of the produced chlorinated polyalkyleneglycol, wherein said polyalkyleneglycol binder is soluble in alcohols, aliphatic solvents and aromatic solvents.
2. The film-forming composition according to claim 1, wherein a catalyst is employed in the chlorination reaction.
3. The film-forming composition according to claim 2, wherein said catalyst is selected from the group consisting of organic peroxides, and diazo compounds.
4. The film-forming composition according to claim 1, wherein the chlorine-resistant solvent is carbon tetrachloride.
5. The film-forming composition according to claim 1, wherein, following the chlorination reaction, the chlorine-resistant solvent is replaced by a desired solvent through a direct solvent displacement process.
6. The film-forming composition according to claim 1, wherein, following the chlorination reaction, the chlorinated polyalkyleneglycol is separated from the solvent by steam distillation, and then dissolved into a desired solvent.
7. The film-forming composition according to claim 2, wherein said catalyst is ultraviolet radiation.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58-70719 | 1983-04-21 | ||
| JP58070719A JPS59196361A (en) | 1983-04-21 | 1983-04-21 | Film-forming composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4539395A true US4539395A (en) | 1985-09-03 |
Family
ID=13439648
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/573,994 Expired - Fee Related US4539395A (en) | 1983-04-21 | 1984-01-26 | Film-forming composition comprising chlorinated polyalkylene glycol |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4539395A (en) |
| JP (1) | JPS59196361A (en) |
| DE (1) | DE3412703A1 (en) |
| FR (1) | FR2544725B1 (en) |
| GB (1) | GB2138833B (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110124761A1 (en) * | 2008-06-10 | 2011-05-26 | Takashi Okada | Chlorinated polyether and polyurethane obtained therefrom |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61190568A (en) * | 1985-01-29 | 1986-08-25 | Sanyo Kokusaku Pulp Co Ltd | High-solid paint composition |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3236786A (en) * | 1962-09-28 | 1966-02-22 | Olin Mathieson | Process for producing chlorinated polyethylene glycol and product so produced |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL107126C (en) * | 1957-06-27 | |||
| BE597240A (en) * | 1959-11-19 | |||
| CA920537A (en) * | 1969-03-05 | 1973-02-06 | E.I. Du Pont De Nemours And Company | Chlorination of organic polymers |
| DE2232540A1 (en) * | 1972-07-03 | 1974-01-24 | Bayer Ag | PROCESS FOR MANUFACTURING HALOGENIC POLYAETHER |
-
1983
- 1983-04-21 JP JP58070719A patent/JPS59196361A/en active Granted
-
1984
- 1984-01-26 US US06/573,994 patent/US4539395A/en not_active Expired - Fee Related
- 1984-01-30 FR FR8401387A patent/FR2544725B1/en not_active Expired
- 1984-02-20 GB GB08404445A patent/GB2138833B/en not_active Expired
- 1984-04-04 DE DE19843412703 patent/DE3412703A1/en active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3236786A (en) * | 1962-09-28 | 1966-02-22 | Olin Mathieson | Process for producing chlorinated polyethylene glycol and product so produced |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110124761A1 (en) * | 2008-06-10 | 2011-05-26 | Takashi Okada | Chlorinated polyether and polyurethane obtained therefrom |
| US8912363B2 (en) | 2008-06-10 | 2014-12-16 | Tosoh Corporation | Chlorinated polyether and polyurethane obtained therefrom |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3412703C2 (en) | 1988-11-17 |
| FR2544725A1 (en) | 1984-10-26 |
| DE3412703A1 (en) | 1984-10-25 |
| GB8404445D0 (en) | 1984-03-28 |
| JPS59196361A (en) | 1984-11-07 |
| FR2544725B1 (en) | 1986-08-08 |
| JPS6238389B2 (en) | 1987-08-18 |
| GB2138833B (en) | 1987-05-20 |
| GB2138833A (en) | 1984-10-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: SANYO-KOKUSAKU PULP CO., LTD., NO. 4-5, MARUNOUCHI Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNORS:SHIMIZU, KZUO;MASAOKA, YOSHIJI;TAKAOKA, MUTSURO;REEL/FRAME:004267/0913 Effective date: 19831223 Owner name: SANYO-KOKUSAKU PULP CO., LTD.,JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SHIMIZU, KZUO;MASAOKA, YOSHIJI;TAKAOKA, MUTSURO;REEL/FRAME:004267/0913 Effective date: 19831223 |
|
| FPAY | Fee payment |
Year of fee payment: 4 |
|
| LAPS | Lapse for failure to pay maintenance fees | ||
| FP | Lapsed due to failure to pay maintenance fee |
Effective date: 19930905 |
|
| STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |